Blood & Tissue

Connecting and leveraging data product lifecycle

2020 Ultimate Guide to Connected Quality Data

Visualizing a new data-centered quality paradigm. When the first Nokia and Motorola cell phones that were affordable and small enough to fit in your pocket hit the market...

WD-40 Company Case Study

WD-40 Company needed a way to ensure that every drop of product produced by globally diverse contract manufacturing organizations (CMOs) measured up to the company’s unwavering standard of quality.

ARUP Laboratories

Efficiency keeps ARUP Laboratories an industry leader.

Top 8 Obstacles in Pharma & Biologics Product Registration & Submission Management

Automation can help pharmaceutical and biologics companies along the path to a global product launch. This white paper identifies common problems with submissions and how best to address them.

Software Automation in the Blood and Biologics Industry

This white paper explores the range of software solutions targeting organizations in the blood and biologics industry, from EDMS to QMS. Evaluate and select the most suitable solution for them.

Compliance with FDA's Good Tissue Practices

This Q&A breaks down the key requirements of 21 CFR Part 1270 (Human Tissue Intended for Transplantation) and Part 1271 (Human Cells, Tissues, and Cellular Tissue-Based Products).

MasterControl Registrations™ Toolkit for Pharma & Biologics Companies

MasterControl Registrations for eCTD is a cloud-based solution designed to streamline content generation and the collection and management of artifacts required for regulatory submission.

Common Reasons for FDA 483 Inspectional Observations in Biologics Manufacturing Environments

Learn about the most common 483 observations and audit findings, and avoid warning letters by staying compliant and addressing issues in the stipulated time period.